2013
DOI: 10.1016/j.saa.2013.06.062
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Binding analysis for interaction of diacetylcurcumin with β-casein nanoparticles by using fluorescence spectroscopy and molecular docking calculations

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Cited by 23 publications
(12 citation statements)
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“…124 Enhanced cytotoxic effect in MCF-7 cells and increased solubility, bioavailability, and anti-tumour activities were observed in a complex composed of a curcumin derivative, Diacetylcurcumin (DAC), and a micellular nanoparticle β-casein. 125 Francis et al 126 created an optimized protocol to produce bis-demethoxy curcumin analogue nanoparticles (BDMCA-NP) that exhibit good anti-cancer therapeutic activities against MCF-7 cells. BDMCA-NPs effectively demonstrated anti-cancer activity by increased apoptosis, G2/M cell cycle arrest, cell death induction through the mitochondrial pathway, and the disassembly of the mitotic spindle of breast cancer cells.…”
Section: The Effect Of Curcumin On Various Breast Cancer Signaling Pamentioning
confidence: 99%
“…124 Enhanced cytotoxic effect in MCF-7 cells and increased solubility, bioavailability, and anti-tumour activities were observed in a complex composed of a curcumin derivative, Diacetylcurcumin (DAC), and a micellular nanoparticle β-casein. 125 Francis et al 126 created an optimized protocol to produce bis-demethoxy curcumin analogue nanoparticles (BDMCA-NP) that exhibit good anti-cancer therapeutic activities against MCF-7 cells. BDMCA-NPs effectively demonstrated anti-cancer activity by increased apoptosis, G2/M cell cycle arrest, cell death induction through the mitochondrial pathway, and the disassembly of the mitotic spindle of breast cancer cells.…”
Section: The Effect Of Curcumin On Various Breast Cancer Signaling Pamentioning
confidence: 99%
“…Docking experiments were carried out to visualize the binding site of BIM to α-casein. All the docking calculations were performed using Autodock 4.2 Tools [33,34] . The macromolecule was kept rigid, while all the torsional bonds of ligands were set free to rotate.…”
Section: Molecular Dockingmentioning
confidence: 99%
“…Eqs. (7)-(9) made it possible to calculate that R o ¼ 3:30 nm, r ¼ 2:78 nm, J ¼ 8:11 Â 10 À15 cm 3 mol À1 L. The distance between the donor and acceptor ðrÞ is less than 7 nm, indicating that the mechanism of energy transfer for quenching is non-radiative [33,34] . The short distance values suggested a strong interaction between BIM and tryptophan residues in β-casein.…”
Section: Energy Transfermentioning
confidence: 99%
“…The amphiphilic nature of β‐casein at neutral pH values causes it to assemble into micelles through self‐association. A single β‐casein molecule has a radius of gyration of 4.6 nm and an isoelectric pH of 5.33 (Mehranfar et al ., ), while micelles consisting of 15–60 β‐casein molecules have Rg values of 7.3–13.5 nm (Mehranfar et al ., ). It has been reported that due to its ‘natively unfolded’ structure, casein protein is more stable to heating than whey protein and that the extent of dissociation or aggregation of casein protein from micelles depends on the temperature and duration of heat treatment (Qi et al ., ; Rahimi Yazdi & Corredig, ; Pinto et al ., ).…”
Section: Introductionmentioning
confidence: 99%